FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH

K Number: K111121 · Decision May 13, 2011
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
6
Review Days
22

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH
K Number
K111121
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Proxy Biomedical , Ltd.
Date Received
April 21, 2011
Decision Date
May 13, 2011
Product Code
FTL
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FTL Mesh, Surgical, Polymeric

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FTL), ordered by most recent decision date.

View all

Other Clearances by Proxy Biomedical , Ltd.

K Number Device Name
K172636 VitaMESH Macroporous PP Surgical Mesh
K060520 VITAMESH MACROPOROUS PP SURGICAL MESH
K052100 MODIFICATION TO MOTIFMESH SOFT TISSUE PATCH
K051245 POLYFORM SYNTHETIC MESH
K050678 MOTIFMESH SOFT TISSUE PATCH